Homo sapiens PMS1 homolog 2, mismatch repair system component (PMS2), - Nucleotide

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Genotype-phenotype correlations in carriers of the PMS2 founder variant c.1831dup. [Mol Genet Genomic Med. 2024]
Genotype-phenotype correlations in carriers of the PMS2 founder variant c.1831dup.
Gass M, Seebauer B, Thommen A, Fischler A, Heinimann K. Mol Genet Genomic Med. 2024 Jan; 12(1):e2360.
PMS2 or PMS2CL? Characterization of variants detected in the 3' of the PMS2 gene. [Genes Chromosomes Cancer. 2024]
PMS2 or PMS2CL? Characterization of variants detected in the 3' of the PMS2 gene.
Bouras A, Lefol C, Ruano E, Grand-Masson C, Wang Q. Genes Chromosomes Cancer. 2024 Jan; 63(1):e23193. Epub 2023 Aug 3.
The p97/VCP segregase is essential for arsenic-induced degradation of PML and PML-RARA. [J Cell Biol. 2023]
The p97/VCP segregase is essential for arsenic-induced degradation of PML and PML-RARA.
Jaffray EG, Tatham MH, Mojsa B, Liczmanska M, Rojas-Fernandez A, Yin Y, Ball G, Hay RT. J Cell Biol. 2023 Apr 3; 222(4). Epub 2023 Feb 28.

RefSeq alternative splicing
See 75 reference mRNA sequence splice variants for the PMS2 gene.
RefSeq protein product
See the reference protein sequence for mismatch repair endonuclease PMS2 isoform d (NP_001308937.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide